Details for New Drug Application (NDA): 208682
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The generic ingredient in MOXIFLOXACIN HYDROCHLORIDE is moxifloxacin hydrochloride. There are eighteen drug master file entries for this compound. Thirty-three suppliers are listed for this compound. Additional details are available on the moxifloxacin hydrochloride profile page.
Summary for 208682
| Tradename: | MOXIFLOXACIN HYDROCHLORIDE |
| Applicant: | Msn |
| Ingredient: | moxifloxacin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 208682
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| MOXIFLOXACIN HYDROCHLORIDE | moxifloxacin hydrochloride | TABLET;ORAL | 208682 | ANDA | REMEDYREPACK INC. | 70518-4312 | 70518-4312-0 | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0) |
| MOXIFLOXACIN HYDROCHLORIDE | moxifloxacin hydrochloride | TABLET;ORAL | 208682 | ANDA | Novadoz Pharmaceuticals LLC | 72205-001 | 72205-001-05 | 500 TABLET, FILM COATED in 1 BOTTLE (72205-001-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 400MG BASE | ||||
| Approval Date: | Sep 22, 2017 | TE: | AB | RLD: | No | ||||
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